The following data is part of a premarket notification filed by Cilco, Inc. with the FDA for Iol Forceps.
| Device ID | K821381 |
| 510k Number | K821381 |
| Device Name: | IOL FORCEPS |
| Classification | Lens, Guide, Intraocular |
| Applicant | CILCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KYB |
| CFR Regulation Number | 886.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-10 |
| Decision Date | 1982-06-14 |